Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
ATP and Macromolecule Synthesis01:28

ATP and Macromolecule Synthesis

Biological macromolecules are organic compounds, predominantly composed of carbon atoms. The carbon atoms are covalently bonded with hydrogen, oxygen, nitrogen, and other minor elements. There are four major biological macromolecule classes: carbohydrates, lipids, proteins, and nucleic acids.
Most macromolecules are composed of single subunits, or building blocks, called monomers. The monomers combine with each other using covalent bonds to form larger molecules known as polymers.
Conversion of...

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Enhanced Diffusion and Retention of Proteoglycan Replacements in Cartilage through Thermoresponsive Polyelectrolytes.

Macromolecules·2026
Same author

3D-Printable Nanoporous Thermosets via Disulfide-Based Polymerization-Induced Microphase Separation.

Angewandte Chemie (International ed. in English)·2026
Same author

Fine structural tuning of the assembly of elastin-collagen peptide conjugates with drug loading and manipulation of molecular interactions.

Biomaterials science·2026
Same author

Light-Programmable Morphology in Photothermal Polyurethanes Based on Stenhouse Salt as Photothermal Agent.

Journal of the American Chemical Society·2026
Same author

From Lipoic Acid to 1,2-Dithianes: Expanding Radical Ring-Opening to Less-Activated Monomers Such as Vinyl Acetate.

Journal of the American Chemical Society·2026
Same author

Topology-Dependent Polymer Stretching and Scission in Solution at Extreme Shear Rates.

ACS polymers Au·2026

関連する実験動画

Updated: Jun 20, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

ブロックコポリマーの自己組み立てを酵素で誘発する.

Roey J Amir1, Sheng Zhong, Darrin J Pochan

  • 1Materials Research Laboratory and Department of Materials, University of California, Santa Barbara, California 93106, USA. ramir@mrl.ucsb.edu

Journal of the American Chemical Society
|September 11, 2009
PubMed
まとめ

ポリマーの酵素活性化は,水溶性物質をアンフィフィリック物質に変えて,高度なアプリケーションのためのナノ構造体への制御された自己組み立てを可能にします.

科学分野:

  • ポリマー化学のポリマー化学について
  • バイオマテリアル科学 バイオマテリアル科学
  • ナノテクノロジー ナノテクノロジー

背景:

  • ダブルヒドロフィリックブロックコポリマーは,ビニルモノマーと割れる酵素基板を使用して合成されます.
  • これらの共ポリマーは,最初は水溶性である.
  • 酵素活性化は,物質特性変化の重要なトリガーです.

研究 の 目的:

  • ダブルヒドロフィリックブロックコポリマーの酵素変換を調査する.
  • 活性化コポリマーがナノ構造に自己組み立てられることを探求する.
  • 酵素誘発物質変化の潜在的応用を強調する.

主な方法:

  • 酵素基板によるビニルモノメアのポリメリゼーション.
  • 結果となる二重ブロック共ポリマーの酵素活性化.
  • コポリマーの特性と自己組み立て行動の特徴化.

主要な成果:

  • 酵素活性化により,当初水溶性であったコポリマーがアンフィフィリックになる.
  • 活性化コポリマーは,自己組織化してコロイドナノ構造を形成します.
  • このプロセスは,材料特性の制御された変化を可能にします.

さらに関連する動画

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
09:02

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

Published on: July 9, 2015

関連する実験動画

Last Updated: Jun 20, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
09:02

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

Published on: July 9, 2015

結論:

  • 酵素活性化により,ポリマーの性質とナノ構造の形成を制御する方法が提供されます.
  • このアプローチは,酵素トリガーされた表面活性化やin vivoナノ構造の形成などの新しいアプリケーションを可能にします.